Ventricular late potentials and myocardial fibrosis in hypertrophic cardiomyopathy

Ayumi Matsuki1, Tatsuya Kawasaki2, Hirofumi Kawamata2

  • 1Department of Cardiology, Matsushita Memorial Hospital, Osaka, Japan; Department of Cardiovascular Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

Insights

Ventricular late potentials (VLPs) are not reliable for detecting myocardial fibrosis in hypertrophic cardiomyopathy (HCM) patients. Cardiac magnetic resonance (CMR) is a more accurate method for assessing fibrosis in this population.

Area of Science:

  • Cardiology
  • Biomedical Engineering

Background:

  • Ventricular late potentials (VLPs) reflect delayed cardiac conduction, often linked to myocardial fibrosis.
  • Hypertrophic cardiomyopathy (HCM) is a condition characterized by myocardial fibrosis and electrical abnormalities.

Purpose of the Study:

  • To investigate the relationship between signal-averaged electrocardiography (SAECG) findings, specifically VLPs, and myocardial fibrosis assessed by cardiac magnetic resonance (CMR) in HCM patients.

Main Methods:

  • The study included 41 HCM patients in sinus rhythm who underwent SAECG (measuring VLPs, filtered QRS duration, low amplitude signal duration [LAS], and root mean square voltage [RMS]) and CMR.
  • Cardiac magnetic resonance (CMR) utilized late gadolinium enhancement (LGE) to assess myocardial fibrosis.
  • The concordance rate between VLP detection and LGE findings was analyzed.

Main Results:

  • Late gadolinium enhancement (LGE) was detected in 13 patients, and VLPs in 14. SAECG parameters (filtered QRS duration, LAS, RMS, VLPs) did not correlate with LGE.
  • Concordance between LGE and VLPs was observed in 26 patients, with 15 showing discordance.
  • Discordant patients exhibited greater maximum wall thickness, higher LGE volume, and predominant LGE in the interventricular septum and anterior wall compared to concordant patients.

Conclusions:

  • Ventricular late potentials (VLPs) are not a dependable marker for identifying myocardial fibrosis in HCM patients when assessed by LGE on CMR.
  • SAECG, including VLPs, is not a substitute for CMR in the evaluation of myocardial fibrosis in HCM.
Abstract

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